Two blog posts on “Living with Covid”

[vivdunstan]

I read a really interesting blog post from literature professor Martin Paul Eve. He has zero antibodies from the Covid vaccine, because of treatment for arthritis and cerebral vasculitis. He’s understandably concerned about current English Covid policy. Anyway I thought his post was a really good public awareness one. And it may be worth sharing more widely among family and friends to spread awareness. It prompted me to write my own blog post on this topic.

Here is Martin’s blog post:

researchprofessionalnews.co...

And here’s mine inspired by it:

vivsacademicblog.wordpress....

[suzannah16]

It's frightening how we have gone from being high risk to "probably ok". I have lupus with lots of scarring in my lungs from pleurisy and blood clots and only one functioning kidney. I have no way of know whether I have anti bodies. The two things covid seems to go for are lungs and kidneys yet I have no testing or access to emergency covid treatments. It makes me so angry the way disabled people are being treated.

[eh66]

Thank you for sharing. It is the politicians whose attitude that if someone with an existing condition dies of Covid, "it's ok", makes my blood boil. Meanwhile they continue stick their snouts in the trough gorging on donors contributions.